Models of multilocus recombination: nonrandomness in chiasma number and crossover positions.

door Goldgar, D E, Fain, P R
Gepubliceerd in 1988

Two CA-dinucleotide polymorphisms at the COL4A5 (Alport syndrome) gene in Xq22

door Barker, D.F., Cleverly, J., Fain, P.R.
Gepubliceerd in 1992

Refined genetic mapping of X-linked Charcot-Marie-Tooth neuropathy.

door Fain, P. R., Barker, D. F., Chance, P. F.
Gepubliceerd in 1994

Two polymorphic TaqI sites at the human NGFR locus (17q12----17q22).

door Wright, E C, Fain, P R, Barker, D F, Chao, M V
Gepubliceerd in 1989

A moderately frequent HindIII polymorphism at the human NGFR locus (17q12----17q22).

door Wright, E C, Fain, P R, Barker, D F, Chao, M V
Gepubliceerd in 1989

The order of loci in the pericentric region of chromosome 17, based on evidence from physical and genetic breakpoints.

door Fain, P R, Wright, E, Willard, H F, Stephens, K, Barker, D F
Gepubliceerd in 1989

A rare PvuII RFLP at the CRYB1 locus (17q11.2----17q12).

door Barker, D F, Fain, P R, Wright, E C, Nguyen, K, Tsui, L C
Gepubliceerd in 1989

MspI RFLP at CRYB1 locus (17q11.2----17q12).

door Barker, D F, Fain, P R, Wright, E C, Nguyen, K, Tsui, L C
Gepubliceerd in 1989

Refined physical and genetic mapping of the NF1 region on chromosome 17.

door Fain, P R, Goldgar, D E, Wallace, M R, Collins, F S, Wright, E, Nguyen, K, Barker, D F
Gepubliceerd in 1989

Clinical variability of type 1 neurofibromatosis: is there a neurofibromatosis-Noonan syndrome?

door Stern, H J, Saal, H M, Lee, J S, Fain, P R, Goldgar, D E, Rosenbaum, K N, Barker, D F
Gepubliceerd in 1992

Evidence for oligogenic inheritance of type 1 diabetes in a large Bedouin Arab family.

door Verge, C F, Vardi, P, Babu, S, Bao, F, Erlich, H A, Bugawan, T, Tiosano, D, Yu, L, Eisenbarth, G S, Fain, P R
Gepubliceerd in 1998

A mutation causing Alport syndrome with tardive hearing loss is common in the western United States.

door Barker, D. F., Pruchno, C. J., Jiang, X., Atkin, C. L., Stone, E. M., Denison, J. C., Fain, P. R., Gregory, M. C.
Gepubliceerd in 1996

A susceptibility locus on chromosome 6q greatly increases risk lung cancer risk among light and never smokers

door Amos, C.I., Pinney, S. M., Li, Y., Kupert, E, Lee, J, de Andrade, M. A., Yang, P., Schwartz, A.G., Fain, P. R., Gazdar, A., Minna, J., Wiest, J.S., Zeng, D., Rothschild, H., Mandal, D., You, M., Coons, Teresa, Gaba, C., Bailey-Wilson, J.E., Anderson, M.W.
Gepubliceerd in 2010